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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436Generated: October 25, 2026

Ethyl fluoroacetate → N-t-butyl-3-(fluoroacetyl)-2-thiophenesulfonamide

https://huagongshe.com/reaction/1436

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl fluoroacetateHCID 9988—
ReactantAmmonium ChlorideHCID 25517—
Reactant3-bromo-N-tert-butylthiophene-2-sulfonamideHCID 14051925—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductN-t-butyl-3-(fluoroacetyl)-2-thiophenesulfonamideHCID 1969078172%

Reaction Conditions

Temperature-78 °C

Reaction Steps

2.98 g (0.0mole) of N-t-butyl-3-bromo-2-thiophenesulfonamide was dissolved in 50mi of dry tetrahydrofuran and the mixture was cooled to -78° C. under nitrogen gas. To the reaction solution was slowly added dropwise 8.4 ml of n-butyl lithium (2.5N) and then the temperature of the mixture was raised slowly to -20° C. and again cooled to -78° C. 1.2 g (0.011 mole) of ethyl fluoroacetate was added slowly to the reaction mixture. The temperature of the mixture was raised again slowly to -20° C. and then the mixture was stirred for 10 minutes. To the reaction mixture was added 100 ml of 5% aqueous ammonium chloride solution, and then added 100 ml of ethylacetate to separate the organic layer. The extracted organic layer was dried over anhydrous magnesium sulfate and concentrated. The residue was subjeced to column chromatography on silica gel to obtain 2.0 g (Yield: 72%) of the pure title compound as a liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05726127
Source datasetuspto-grants-1998_03
ORD IDord-c8e3bb374a104faca742086988b3b35f
Source noteuspto-grants-1998_03